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Axon Guidance Molecules in the Islets of Langerhans

The islets of Langerhans, responsible for regulating blood glucose in vertebrates, are clusters of endocrine cells distributed throughout the exocrine pancreas. The spatial architecture of the different cell types within the islets controls cell-cell communication and impacts their ability to collec...

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Detalles Bibliográficos
Autores principales: Waters, Bayley J., Blum, Barak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048200/
https://www.ncbi.nlm.nih.gov/pubmed/35498433
http://dx.doi.org/10.3389/fendo.2022.869780
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author Waters, Bayley J.
Blum, Barak
author_facet Waters, Bayley J.
Blum, Barak
author_sort Waters, Bayley J.
collection PubMed
description The islets of Langerhans, responsible for regulating blood glucose in vertebrates, are clusters of endocrine cells distributed throughout the exocrine pancreas. The spatial architecture of the different cell types within the islets controls cell-cell communication and impacts their ability to collectively regulate glucose. Islets rely on a range of chemotactic and adhesive cues to establish and manage intercellular relationships. Growing evidence indicates that axon guidance molecules such as Slit-Robo, Semaphorin-Neuropilin, Ephrin-Eph, and Netrins, influence endocrine progenitors’ cell migration to establish correct architecture during islet morphogenesis, as well as directly regulating physical cell-cell communication in the mature islet to coordinate hormone secretion. In this mini-review, we discuss what is known and not yet known about how axon guidance molecules contribute to islet morphogenesis and function.
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spelling pubmed-90482002022-04-29 Axon Guidance Molecules in the Islets of Langerhans Waters, Bayley J. Blum, Barak Front Endocrinol (Lausanne) Endocrinology The islets of Langerhans, responsible for regulating blood glucose in vertebrates, are clusters of endocrine cells distributed throughout the exocrine pancreas. The spatial architecture of the different cell types within the islets controls cell-cell communication and impacts their ability to collectively regulate glucose. Islets rely on a range of chemotactic and adhesive cues to establish and manage intercellular relationships. Growing evidence indicates that axon guidance molecules such as Slit-Robo, Semaphorin-Neuropilin, Ephrin-Eph, and Netrins, influence endocrine progenitors’ cell migration to establish correct architecture during islet morphogenesis, as well as directly regulating physical cell-cell communication in the mature islet to coordinate hormone secretion. In this mini-review, we discuss what is known and not yet known about how axon guidance molecules contribute to islet morphogenesis and function. Frontiers Media S.A. 2022-04-14 /pmc/articles/PMC9048200/ /pubmed/35498433 http://dx.doi.org/10.3389/fendo.2022.869780 Text en Copyright © 2022 Waters and Blum https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Waters, Bayley J.
Blum, Barak
Axon Guidance Molecules in the Islets of Langerhans
title Axon Guidance Molecules in the Islets of Langerhans
title_full Axon Guidance Molecules in the Islets of Langerhans
title_fullStr Axon Guidance Molecules in the Islets of Langerhans
title_full_unstemmed Axon Guidance Molecules in the Islets of Langerhans
title_short Axon Guidance Molecules in the Islets of Langerhans
title_sort axon guidance molecules in the islets of langerhans
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048200/
https://www.ncbi.nlm.nih.gov/pubmed/35498433
http://dx.doi.org/10.3389/fendo.2022.869780
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